@pausedME I forgot. About the same time I started Abilify I also started medical cannabis for sleep. It’s not a panacea but it helped with better sleep. Perhaps it was both those things plus time.
@pausedME I was bedridden for 12+ years and a couple years ago I slowly started to improve. I’m still recovering but I don’t need a wheelchair anymore. I’d say that I went from severe to moderate. Just wanted to give hope to others.
@VNoelte12@pausedME See my comments under Tim T and Canadian gymnerd. I wish I knew the secret so I help others but the only thing I can think of is starting Abilify about 3-4 yrs ago and time. Some get better after time spontaneously.
@canadiangymnerd@pausedME See my answer under Tim T. I started Abilify about 3-4 yrs ago and that slowly helped. Other than that I haven’t a clue. Dr Lapp in NC said people often start feeling better after 6 years. For me it was twice that long.
@tabler_tim@pausedME It was very slow improvement. I started feeling a bit better after I started taking Abilify but it took about 3-4 years. It still is a very slow and steady improvement. I wish I knew definitively so I could help others.
@NG85522206@pausedME My muscles got very weak but they are building up steadily. I only used the wheelchair for doctor visits and such. I would walk in my bedroom to the bath and back. Now the most I’ve walk so far was equivalent to a block or so. I find my back is the weaker than my legs.
Seven years into my #MECFS journey, I got an appt. with Dr. Montoya's PA, who prescribed 800 mg Acyclovir 3/day (increasing dosage). I was warned of herxing...didn't. Started to see improvement the second week. I got 3.5 months of 'normal' then it just stopped working. No
1/x
I spoke earlier today with @CGATistgeneticist Chris Ponting, a professor at the University of Edinburgh, about his recent piece for The Conversation regarding the plight of ME patients, medical misogyny, and related issues: https://t.co/r2rXFwBMEu